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Nombre Fecha Fecha de inicio País Fuente
Retiro De Equipo (Recall) de Device Recall VasoSeal ES 2003-07-28 United States USFDA
Retiro De Equipo (Recall) de BD Test Strips. || The US market BD Test Strips are identified by Catalog Numbers 322027 (50 count BD Test Strips Durable medical Equipment consignees), 322053 (50 Count BD Test Strips Trade consignees), and 322060 (10 Count BD Test Strips packaged within BGM kits). The Canadian market BD Test Strips are identified by Catalog Numbers 322002 (50 count BD Test Strips), 322003 (100 count BD Test strips), and 322009 (10 count BD Test strips). || Health Hazard Evaluation: There is negligible medical risk to patients with diabetes using the BD blood glucose systems due to the increase of E-3 error messages. 2004-01-29 United States USFDA
Retiro De Equipo (Recall) de Device Recall Cruciform Slit Valve 2004-01-06 United States USFDA
Retiro De Equipo (Recall) de Device Recall One Way Valve/Female to Male Flow 2004-02-03 United States USFDA
Retiro De Equipo (Recall) de Vaxcel Port with PASV Valve, 8 Fr polyurethane catheter, Mini Titanium port, Implantable Port System, Model # M001452150, Catalog #45-215 2004-02-10 United States USFDA
Retiro De Equipo (Recall) de Vaxcel Port with PASV Valve, 8 Fr polyurethane catheter, STD Titanium Port, Implantable Port System, Model # M001453620, Catalog #45-362 2004-02-10 United States USFDA
Retiro De Equipo (Recall) de Vaxcel Port with PASV Valve, 8 Fr polyurethane catheter, Low Profile PS port, Implantable Port System, Model # M001452380, Catalog #45-238 2004-02-10 United States USFDA
Retiro De Equipo (Recall) de Vaxcel Port with PASV Valve, 8 Fr polyurethane catheter, STD PS port, Implantable Port System, Model # M001453660, Catalog #45-366 2004-02-10 United States USFDA
Retiro De Equipo (Recall) de Device Recall Cronus 2004-01-27 United States USFDA
Retiro De Equipo (Recall) de Device Recall Cronus 2004-01-27 United States USFDA
Retiro De Equipo (Recall) de Device Recall Cronus 2004-01-27 United States USFDA
Retiro De Equipo (Recall) de Device Recall HideAPort Low Profile Balloon Gastrostomy Tube Kit 2004-03-01 United States USFDA
Retiro De Equipo (Recall) de Device Recall Cronus 2004-01-27 United States USFDA
Retiro De Equipo (Recall) de Device Recall Cronus 2004-01-27 United States USFDA
Retiro De Equipo (Recall) de Device Recall Stryker Orthopaedics 2004-02-10 United States USFDA
Retiro De Equipo (Recall) de Device Recall General Electric Seneographe 2004-02-06 United States USFDA
Retiro De Equipo (Recall) de Device Recall General Electric Seneographe 2004-02-06 United States USFDA
Retiro De Equipo (Recall) de Device Recall General Electric Seneographe 2004-02-06 United States USFDA
Retiro De Equipo (Recall) de Device Recall General Electric Seneographe 2004-02-06 United States USFDA
Retiro De Equipo (Recall) de Device Recall General Electric Seneographe 2004-02-06 United States USFDA
Retiro De Equipo (Recall) de Device Recall PatientNet 2004-02-27 United States USFDA
Retiro De Equipo (Recall) de Device Recall 3M Attest 2004-02-27 United States USFDA
Retiro De Equipo (Recall) de The BD Blood Glucose Monitoring Systems identified as the BD Latitude, and BD Logic. Becton Dickinson also distributes the Paradigm Link Blood glucose Monitor which is sold exclusively for Medtronic Mini Med. || US Market BD Blood Glucose Monitoring System kit catalog Numbers: || 322025 (BD Logic Blood Glucose Monitor Durable Medical Equipment consignees); || 322050 (BD Latitude Diabetes Management System); || 322051 (BD Logic Blood Glucose Monitor); || 32205175 ( BD Logic Blood Glucose Monitor); || 322200 (Paradigm Link Blood Glucose Monitor - clear); || 322201 ( Paradigm Link Blood Glucose Monitor - smoke); || 322202 (Paradigm Link Blood Glucose Monitor - blue); || 322203 (Paradigm Link Blood Glucose Monitor - purple). || Canadian market BD Blood Glucose Monitoring System kit catalog numbers: || 322000 (BD Latitude Diabetes Management System); || 322001 (BD Logic Blood Glucose Monitor). 2004-01-29 United States USFDA
Retiro De Equipo (Recall) de Device Recall Salvart Oral Moisturizer 2004-02-23 United States USFDA
Retiro De Equipo (Recall) de Device Recall AngioDynamics 2004-02-26 United States USFDA